Information recording medium

ABSTRACT

Disclosed is an information recording medium having a recording layer which contains a phenol type compound. This information recording medium therefore exhibits very excellent effects in light resistance and is safe to use.

This is a Continuation of application Ser. No. 08/106,552 filed Aug. 16, 1993, now abandoned.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a writable information recording medium, and, more particularly, to an information recording medium having a recording layer and a reflective layer formed on a substrate having light transmission properties.

2. Description of the Related Art

It is known that conventional writable information recording media use a recording layer essentially consisting of an organic dye, such as a cyanine type dye or a phthalocyanine type dye.

To write information on such an information recording medium, a laser beam is focused on a minute area of the recording layer so that it is transferred to thermal energy to alter the property of the recording layer, thus accomplishing the information recording (forming pits). To smoothly change the property of the recording layer, the information recording media typically employ a so-called air sandwich structure which is accomplished by preparing two sets of substrate-and-recording-layer laminations each having a recording layer formed on a transparent substrate, and arranging those two sets of lamination structures in such a way that the recording layers face each other.

A write laser beam used for this type of information recording medium is irradiated on this medium from the transparent substrate side to form optically readable pits in the recording layer. A read laser beam for reproducing the recorded data has a lower intensity than the write laser beam. When this read laser is irradiated on the information recording medium, the contrast between a pit-formed portion and a pit-absent portion is read out as an electrical signal.

There is a different type of medium on which data has been pre-recorded, a so-called ROM (Read Only Memory) type medium. The ROM type media are widely used in the fields of audio recording and information processing. This type of medium however does not have the writable recording layer mentioned above. More specifically, pre-pits corresponding to data to be reproduced have previously been formed on a plastic substrate by injection molding, and a reflective layer of a metal such as Au, Ag, Cu and Al is formed on the pits-formed substrate, with a protective layer covering the top of the reflective layer. A typical ROM type medium is a so-called CD (Compact Disk). The specifications for recording and reading signals for this CD are standardized, and compact disk players (CD players), which conform to the standards, are widely used as CD reproducing apparatuses.

The aforementioned writable information recording medium is the same as a CD in the use of a laser beam and in its disk shape. There is therefore a strong demand for the development of writable media, which conform to the standards of the CD specifications and can be thus used directly in available CD players. To meet this demand, actual samples have been gradually proposed.

An organic dye, which is the essential component in the recording layer of such a writable information recording medium, does not have sufficient light resistance. Nitroso compounds which prevent tenebrescence are used as one means to improve the light resistance.

However, there is a strong demand for media whose recording layer contains a material that is much safer and easier to be synthesized than those of a nitroso compound and further having an excellent effect of improving light resistance.

SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to overcome the aforementioned shortcomings and to provide a writable information recording medium which is very safe to use and has excellent light resistance.

To achieve the foregoing and other objects and in accordance with the object of the present invention, there is provided an information recording medium having a recording layer formed on a substrate and a reflective layer formed on the recording layer, the recording layer containing at least one cyanine dye selected from those represented by the general formulae [I] and [II] given later, and a phenol type compound represented by the general formula [III] also given later.

A specific constitution of the present invention will be described in detail below in conjunction with the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic partly cutaway perspective view of an information recording medium according to the present invention; and

FIG. 2 is a partly enlarged cross section of the cutaway portion in FIG. 1.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

An information recording medium 1 according to the present invention has a recording layer 12 formed on a substrate 11 having light transmission properties and a light-reflective layer 13 formed on the recording layer 12, with a protective layer 14 disposed on the light-reflective layer 13.

The recording layer 12 formed on the substrate 11 contains at least one type of cyanine dye selected from those represented by the following general formulae [I] and [II]. ##STR1## wherein R₁ and R₂ each represent an alkyl group having 1 to 8 carbon atoms, preferably 3 to 5 carbon atoms. When the number of carbon atoms exceeds 8, this cyanine dye becomes difficult to handle. In general formula [I], X⁻ represents a counter ion which typically includes ClO₄ ⁻, I⁻, B⁻ or the like. ##STR2## wherein R₃ and R₄ each represent an alkyl group having 1 to 8 carbon atoms, preferably 3 to 5 carbon atoms. When the number of carbon atoms exceeds 8, the same problem arises as that in general formula [I]. X⁻ represents a counter ion, which is the same as the one defined for the formula [I].

While cyanine dyes represented by the general formulae [I] and [II] may be used singularly, it is preferable to use a mixture of a cyanine dye represented by the general formula [I] and another cyanine dye represented by the general formula [II] in order to assure high reflectance, recording sensitivity and good modulation of the recorded signals. When a mixture of the cyanine dyes is used, the mixing ratio is 100 to 300 parts by weight of the cyanine dye represented by the general formula [II] with respect to 100 parts by weight of the cyanine dye represented by the general formula [I].

The recording layer 12 further contains a phenol type compound represented by the following general formula [III] or [IV] to prevent light degradation (fading) of the aforementioned cyanine dye: ##STR3## wherein R₅ and R₆ independently represent a hydrogen, halogen such as chlorine or a substituted or unsubstituted alkyl or alkoxy group having 1 to 8 carbon atoms, preferably 1 to 4 carbon atoms, and q1 and q2 independently represent integers 1 to 5, preferably 1 to 3, and P1 and P2 independently represent integers 0 to 5, preferably 1 to 3. It is necessary for such integers to suffer relationships q1+P1≦6 and q2+P2≦5. When each of P1 and P2 is 2 or more the substituents for R₅ and R₆ may be the same or different from one another. In formula [III], Y represents one of connecting groups such as the following formulae [Y-1] to [Y-4]. ##STR4##

The other phenol type compound in the recording layer is represented by the following general formula [IV]. ##STR5## wherein R₇, R₈ and R₉ independently represent hydrogen, halogen such as chlorine or a substituted or unsubstituted alkyl or alkoxy group having 1 to 8 carbon atoms, preferably 1 to 4 carbon atoms, and q3, q4 and q5 independently represent integers 1 to 5, preferably 1 to 3, and P3, P4 and P5 independently represent integers 0 to 5, preferably, preferably 1 to 3. It is necessary for the integers to suffer relationships q3+P3≦5 and q4+P4≦5 and q5+P5≦5. When each of P3, P4 and P5 is 2 or more the substituents for R₇, R₈ and R₉ may be the same or different from one another. In formula [IV], L represents a connecting groups represented by the following formula [L-1]. ##STR6##

A specific example of the phenol type compound include materials represented by the following structural formulae [PH-1] and [PH-2]. ##STR7##

Such phenol type compound is contained in an amount of 5 to 50 parts by weight, preferably 20 to 25 parts by weight relative to 100 parts by weight of the aforementioned cyanine dye. When this value exceeds 50 parts by weight, the recording sensitivity undesirably drops, whereas when the value becomes less than 5 parts by weight, the effect of improving light resistance undesirably decreases.

The recording layer may contain a plurality of these phenol type compounds.

The recording layer 12 may further contain a quencher in addition to the phenol type compound, particularly, a Ni complex represented by the following general formula [V]. ##STR8## wherein R₁₀ to R₁₃ each represent hydrogen or its substituent. Examples of the substituent include CH₃ O--, CH₃ OCH₂ CH₂ O--, CH₃ COO--, (n--C₃ H₇)₂ N--, (C₂ H₅)₂ N-- and Cl--.

Specific examples of such a quencher include, for example, those represented by the following structural formulae [Q-1] to [Q-4]. Among them, the one represented by the structural formula [Q-1] is preferred. ##STR9##

The recording layer 12 containing the aforementioned cyanine dye and phenol type compound is applied on the substrate 11 by typical means such as spin coating.

The thickness of the recording layer 12 to be coated is 30 to 900 nm, preferably 100 to 300 nm. When the thickness becomes less than 30 nm, light absorption is reduced so that the sensitivity in the wavelength of the semiconductor laser lowers, disabling the recording of signals. When the thickness exceeds 900 nm, the dye becomes thick which causes an increase in the light absorption while undesirably reducing the reflectance.

Various types of known solvents can be used for coating the recording layer 12; they include diacetone alcohol, ethyl cellosolve, methyl cellosolve, isophorone, methanol and tetrafluoropropanol.

The substrate 11 on which this recording layer 12 is applied, generally, has a disk shape. From the view point of improving the productivity, it is preferable to use an integrally formed injection-molded resin substrate as the substrate 11. This substrate may be formed of a transparent material, such as polycarbonate resins (PC) or polymethyl methacrylate (PMMA). Particularly, it is preferred to use polycarbonate resins (PC) with an average molecular weight of 32,000 to 40,000. The substrate 11 is not limited to such integrally formed injection-molded resin substrate, but may be formed by the 2P (photo-polymer) method. The thickness of the thus formed substrate 11 is about 1.0 to 1.5 mm.

The light-reflective layer 13 is provided on the recording layer 12 coated on the substrate 11. The light-reflective layer 13 is formed of a metal such as Au, Ag, Cu or Al, and the film-formation is carried out by vacuum vapor deposition, sputtering, ion plating or the like. The thickness of the light-reflective layer 13 is about 0.02 to 2.0 μm.

The protective layer 14 is usually provided on the light-reflective layer 13 to protect the recording layer (light-absorbing layer) 12 and the light-reflective layer 13. In general, the protective layer 14 is formed by coating an ultraviolet-hardening resin on the light-reflective layer 13 by spin coating and then irradiating ultraviolet rays on the resultant structure to harden the coated film. Other possible materials for the protective layer 14 include epoxy resins, acrylic resins, silicone resins and urethane resins. The thickness of the protective layer 14 is generally about 0.1 to 100 μm.

An intermediate layer may be provided between the substrate 11 and the light-absorbing layer 12 to protect the substrate 11 from the solvent. An intermediate layer may be provided between the light-absorbing layer 12 and the light-reflective layer 13 to improve efficiency for the light absorption.

The wavelength of light used for information recording and reproduction in the present invention is about 780 to 830 μm.

The present invention will be described in more detail by way of specific examples.

[Preparation of Sample 1 of the Present Invention]

The following two types of cyanine dyes [D-1] and [D-2] were used as the cyanine dyes contained in the recording layer, and the aforementioned material [PH-1] was used as the phenol type compound. The mixing ratio (parts by weight) of these components was [D-1]:[D-2]: [PH-1]=100:180:65.

Cyanine Dye [D-1]

In the aforementioned general formula [I], R₁ and R₂ each were n--C₄ H₉, and X⁻ was ClO₄ ⁻.

Cyanine Dye [D-2]

In the aforementioned general formula [II], R₃ and R₄ each were n--C₃ H₇, and X⁻ was I⁻.

Those dyes and phenol type compound were dissolved in a solvent (1000 parts by weight) of ethyl cellosolve, and the resulting solution was coated 120 nm thick on an acrylic substrate 120 mm in diameter and 1.2 mm in thickness.

[Preparation of Sample 2 of the Present Invention]

Sample 2 of the present invention was prepared in the same manner as Sample 1 except that the phenol type compound [PH-1] was substituted with [PH-2].

[Preparation of Sample 3 of the Present Invention]

Sample 3 of the present invention was prepared in the same manner as Sample 1 except that the aforementioned quencher [Q-1] was added to the composition of the recording layer used in Sample 1. The mixing ratio (parts by weight) of the components was [D-1]:[D-2]:[PH-1]:[Q-1]=100:180:65:40.

[Preparation of Sample 4 of the Present Invention]

Sample 4 of the present invention was prepared in the same manner as Sample 2 except that the aforementioned quencher [Q-1] was added to the composition of the recording layer used in Sample 2. The mixing ratio (parts by weight) of the components was D-1]:[D-2]:[PH-2]:[Q-1]=100:180:65:40.

Preparation of Comparative Sample 1]

Comparative Sample 1 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with bis(1,2,2,6,6-pentamethyl-4-piperidyl)-2-(3,5-di-t-butyl-hydroxybenzyl)-2-n-butyl malonate compound represented by the following structural formula [C-1]. ##STR10##

Preparation of Comparative Sample 2]

Comparative Sample 2 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate compound represented by the following structural formula [C-2]. ##STR11##

Preparation of Comparative Sample 3]

Comparative Sample 3 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with a compound represented by the following structural formula [C-3]. ##STR12##

Preparation of Comparative Sample 4]

Comparative Sample 4 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with a compound represented by the following structural formula [C-4]. ##STR13##

Preparation of Comparative Sample 5]

Comparative Sample 5 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with a compound represented by the following structural formula [C-5]. ##STR14##

[Preparation of Comparative Sample 6]

Comparative Sample 6 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with a compound represented by the following structural formula [C-6]. ##STR15##

[Preparation of Comparative Sample 7]

Comparative Sample 7 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was replaced with a compound represented by the following structural formula [C-7]. ##STR16##

[Preparation of Comparative Sample 8]

Comparative Sample 8 was prepared in the same manner as in Sample 1 of the present invention except that the phenol type compound [PH-1] was eliminated.

[Preparation of Comparative Sample 9]

Comparative Sample 9 was prepared in the same manner as in Sample 2 of the present invention except that the phenol type compound [PH-1] was eliminated.

A light resistance test was conducted for the above Samples 1 and 2 of the present invention and Comparative Samples 1 to 9 in the following manner.

[Light Resistance Test]

Light from a cool white fluorescent lamp (40 W) was continuously irradiated on those samples for 30 hours at a distance of 10 cm.

Then, the transmittance in each sample was measured and the fading ratio (%)=(transmittance after 30 hours/initial transmittance)×100 was computed. This value of the fading ratio was evaluated as follows: 0 to less than 7% marked "o" (very good), 7 to less than 10% marked "Δ" (not good enough) and above 10% marked "X" (impractical).

                  TABLE 1                                                          ______________________________________                                         Sample No.     Result of Light Resistance Test                                 ______________________________________                                         Sample 1 of the                                                                               ◯ (4.9%)                                            present invention                                                              Sample 2 of the                                                                               ◯ (4.0%)                                            present invention                                                              Sample 3 of the                                                                               ◯ (4.8%)                                            present invention                                                              Sample 4 of the                                                                               ◯ (3.8%)                                            present invention                                                              Comparative Sample 1                                                                          Δ ( 7.5%)                                                 Comparative Sample 2                                                                          X (14.0%)                                                       Comparative Sample 3                                                                          Δ ( 7.3%)                                                 Comparative Sample 4                                                                          X (12.8%)                                                       Comparative Sample 5                                                                          Δ ( 7.0%)                                                 Comparative Sample 6                                                                          Δ (8.9%)                                                  Comparative Sample 7                                                                          X (10.2%)                                                       Comparative Sample 8                                                                          X (10.0%)                                                       Comparative Sample 9                                                                          X ( 9.7%)                                                       ______________________________________                                    

The values in the parentheses indicate the fading ratios. 

What is claimed is:
 1. An information recording medium having a disk shape comprising: a transparent substrate having a disk shape; a recording layer formed on said substrate; and a reflective layer formed on said recording layer, wherein said recording layer consists of at least one cyanine dye represented by formula (I) or (II), and a phenol type compound represented by formula (PH-1) or (PH-2): ##STR17## wherein R₁ and R₂ each represent an alkyl group having 1 to 8 carbon atoms, and X⁻ represents a counter ion; ##STR18## wherein R₃ and R₄ each represent an alkyl group having 1 to 8 carbon atoms, and X⁻ represents a counter ion; ##STR19## wherein said phenol type compound is present in an amount of 5 to 50 parts by weight relative to 100 parts by weight of said cyanine dye.
 2. The information recording medium according to claim 1, wherein said recording layer contains two cyanine dyes represented by the general formulae (I) and (II) respectively, wherein R₁ and R₂ in formula (I) are each n--C₄ H₉ and X⁻ is ClO₄ ⁻, and R₃ and R₄ in formula (II) are each n--C₃ H₇ and X is I⁻.
 3. The information recording medium according to claim 1, wherein said recording layer further contains a quencher of a Ni complex selected from the group consisting of structural formulae (Q-1) to (Q-4), ##STR20## 